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Presenilin 1 Regulates Membrane Homeostatic Pathways that are Dysregulated in Alzheimer’s Disease

Mutations in the PSEN1 gene, encoding presenilin 1 (PS1), are the most common cause of familial Alzheimer’s disease(fAD). Since the first mutations in the PSEN1 gene were discovered more than 25 years ago, many postulated functions of PS1 have been investigated. The majority of earlier studies focus...

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Podrobná bibliografie
Vydáno v:J Alzheimers Dis
Hlavní autoři: Deaton, Carol A., Johnson, Gail V.W.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2020
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8056533/
https://ncbi.nlm.nih.gov/pubmed/32804090
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JAD-200598
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